Periventricular Heterotopia With Microcephaly, Autosomal Recessive

Alternative Names

  • ARPHM
  • Periventricular Nodular Heterotopia 2
  • PVNH2
  • Heterotopia, Periventricular, Autosomal Recessive
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WHO-ICD-10 version:2010

Congenital malformations, deformations and chromosomal abnormalities

Congenital malformations of the nervous system

OMIM Number

608097

Mode of Inheritance

Autosomal recessive

Gene Map Locus

20q13.13

Description

Periventricular nodular heterotopia is a disorder of neuronal migration in which neurons fail to migrate appropriately from the ventricular zone to the cortex during development, resulting in the formation of nodular brain tissue lining the ventricles. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
608097.1.1EgyptMaleYesYes Severe global developmental delay; Autis...NM_006420.3:c.2776C>THomozygousAutosomal, RecessiveMakrythanasis et al. 2014
608097.1.2EgyptMaleYesYes Severe global developmental delay; Autis...NM_006420.3:c.2776C>THomozygousAutosomal, RecessiveMakrythanasis et al. 2014 Second-cousin of 608...
608097.2Saudi Arabia Global developmental delay; Seizure; Hyd...NM_006420.3:c.656dupHomozygousAutosomal, RecessiveAlazami et al. 2015
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